@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_head
{
this:
np:hasAssertion
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_assertion
;
np:hasProvenance
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_provenance
;
np:hasPublicationInfo
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_assertion
a
np:Assertion
.
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_provenance
a
np:Provenance
.
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN806dc42b0e3c5cdbb62c57dcdc450a68
sio:SIO_000628
miriam-gene:1493
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_provenance
{
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_assertion
dcterms:description
"[These data suggested ICOS polymorphism could affect the susceptibility to AMD by elevating protein expression, and serum levels of sICOS may be closed correlated with the development and progression of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:24083358
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP731762.RA0Cp35Pz07f9wylm44NxbxeYnusFQS40hs4Z0-W6oWso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}